Rückinger Simon, von Kries Rüdiger, Siedler Annette, van der Linden Mark
Institute of Social Pediatrics and Adolescent Medicine, Ludwig-Maximilians-University of Munich, Munich, Germany.
Pediatr Infect Dis J. 2009 Feb;28(2):118-22. doi: 10.1097/INF.0b013e318187e215.
Invasive pneumococcal disease (IPD) in children may manifest as bacteremia/sepsis, bacteremic pneumonia, or meningitis, with serious outcomes that include hospitalization, neurologic sequelae, or death. The risk of severe or fatal outcome of disease is associated with host-related factors, such as age or comorbid conditions. Furthermore, there is an ongoing discussion about organism-related factors, such as the pneumococcal serotype.
Data on 494 children aged <16 years hospitalized for IPD between 1997 and 2003 in pediatric hospitals in Germany were analyzed. Serotype specific case-fatality rates and rates of severe outcome were compared using standardized mortality ratios (SMR). The risk of severe or fatal outcome for the serotype with the highest case-fatality rate was further analyzed using multivariate logistic regression adjusting for age younger than 1 year, meningitis, sex, and immunocompromised status as potential confounders.
The overall case-fatality rate was 5.3% and the rate of severe outcome was 17.0%. Serotype 7F had the highest case-fatality rate (14.8%, SMR 3.1), followed by serotypes 23F (8.3%, SMR 1.7) and 3 (8.3%, SMR 1.7). The highest rate of severe outcome was also observed for 7F (40.7%, SMR 2.4). Multivariate analysis showed an odds ratio of 4.3 (1.3-14.7) for fatal outcome and 4.0 (1.6-10.4) for severe outcome comparing 7F to all other serotypes.
In this study population, serotype 7F accounted for a higher risk of severe and fatal outcome than other serotypes of Streptococcus pneumoniae. In describing the epidemiology of IPD, the serotype-specific risk for severe or fatal outcome is an important complement to other serotype-specific aspects like incidence and antibiotic resistance pattern.
儿童侵袭性肺炎球菌疾病(IPD)可表现为菌血症/败血症、菌血症性肺炎或脑膜炎,严重后果包括住院、神经后遗症或死亡。疾病严重或致命后果的风险与宿主相关因素有关,如年龄或合并症。此外,关于病原体相关因素,如肺炎球菌血清型,也存在持续的讨论。
分析了1997年至2003年期间在德国儿科医院因IPD住院的494名16岁以下儿童的数据。使用标准化死亡率(SMR)比较血清型特异性病死率和严重后果发生率。对病死率最高的血清型,进一步采用多因素逻辑回归分析严重或致命后果的风险,调整年龄小于1岁、脑膜炎、性别和免疫功能低下状态作为潜在混杂因素。
总体病死率为5.3%,严重后果发生率为17.0%。7F血清型病死率最高(14.8%,SMR 3.1),其次是23F血清型(8.3%,SMR 1.7)和3血清型(8.3%,SMR 1.7)。7F血清型严重后果发生率也最高(40.7%,SMR 2.4)。多因素分析显示,7F血清型与所有其他血清型相比,致命后果的优势比为4.3(1.3 - 14.7),严重后果的优势比为4.0(1.6 - 10.4)。
在本研究人群中,7F血清型比其他肺炎链球菌血清型导致严重和致命后果的风险更高。在描述IPD的流行病学特征时,血清型特异性的严重或致命后果风险是对其他血清型特异性方面(如发病率和抗生素耐药模式)的重要补充。